ClinVar Miner

Submissions for variant NM_000328.3(RPGR):c.1905+479del (rs1569237206)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Human Genetics - Radboudumc,Radboudumc RCV000678621 SCV000804709 pathogenic Retinitis pigmentosa 15 2016-09-01 no assertion criteria provided clinical testing
Molecular Diagnostics Laboratory,M Health: University of Minnesota RCV000761348 SCV000891334 likely pathogenic Retinitis pigmentosa 2018-05-04 criteria provided, single submitter clinical testing

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